Good Documentation Practices (GDP) in Pharmaceutical Industry document contains the the instructions which are required to be followed for compliance of Good Documentation Practices (GDP) during preparation,...

This Book contains regarding Pharmaceutical Quality Management System (QMS) and its related guidelines as well as the Questions and Answers of Change control, Deviation and Corrective Action and Preventive...

This Book contains 11 Modules of  Current Good Manufacturing Practices (cGMP) requirements for pharmaceutical industry which will be very useful for job seekers in Pharma sector, Beginners and Learners...

Annual Product Quality Review (APQR) is regular periodic or rolling quality reviews of all licensed medicinal products which are conducted with the objective of verifying the consistency of the existing...

CAPA is a systematic approach used by organizations to identify, investigate, and address non- conformances, problems, or issues within their processes, products, or services which plays a vital role...

This Books contain the Role and Responsibility of Pharmaceutical Industry Plant personnel like Quality Assurance, Quality Control, Production, Warehouse, Engineering and Information Technology. This book...

This Book contains the requirement of  site Master File (SMF) in Pharmaceutical Industry  and it is a document that describes the structure of the organization which involved the site, the Manufacturing...

This Book contains the basic requirements which is required in Quality Control Laboratory